Compound Information | SONAR Target prediction |
Name: | Nitrofurantoin |
Unique Identifier: | LAT002B06 |
MolClass: | Checkout models in ver1.5 and ver1.0 |
Molecular Formula: | C8H6N4O5 |
Molecular Weight: | 232.11 g/mol |
X log p: | 6.195 (online calculus) |
Lipinksi Failures | 1 |
TPSA | 102.11 |
Hydrogen Bond Donor Count: | 0 |
Hydrogen Bond Acceptors Count: | 6 |
Rotatable Bond Count: | 3 |
Canonical Smiles: | [O-][N+](=O)c1oc(cc1)C=NN1CC(=O)NC1=O |
Generic_name: | Nitrofurantoin |
Chemical_iupac_name: | 1-[(5-nitro-2-furyl)methylideneamino]imidazolidine-2,4-dione |
Drug_type: | Approved Drug |
Pharmgkb_id: | PA450640 |
Kegg_compound_id: | C07268 |
Drugbank_id: | APRD00191 |
Melting_point: | 263 oC |
H2o_solubility: | 79.5 mg/L |
Logp: | -0.04 |
Isoelectric_point: | 7.2 |
Cas_registry_number: | 67-20-9 |
Mass_spectrum: | http://webbook.nist.gov/cgi/cbook.cgi?Spec=C67209&Index=0&Type=Mass&Large=on |
Drug_category: | Anti-Infectives; Anti-Infectives; ATC:J01XE01 |
Indication: | For the treatment of infection (urinary tract) |
Pharmacology: | Nitrofurantoin, a nitrofuran antibacterial agent, is available in microcrystalline and macrocrystalline form to treat urinary tract infections caused by many gram-negative and some gram-positive bacteria. |
Mechanism_of_action: | Nitrofurantoin inhibits bacterial acetyl-coenzyme A, interfering with the organism-s carbohydrate metabolism. The drug also can disrupt bacterial cell wall formation. |
Organisms_affected: | Gram negative and some gram positive bacteria |